Unique Heme-Iron Coordination by the Hemoglobin Receptor IsdB of

ARTICLE pubs.acs.org/biochemistry

Unique Heme-Iron Coordination by the Hemoglobin Receptor IsdB of Staphylococcus aureus Catherine F. M. Gaudin, Jason C. Grigg, Angele L. Arrieta, and Michael E. P. Murphy* Department of Microbiology and Immunology, Life Sciences Institute, The University of British Columbia, Vancouver, BC, Canada V6T 1Z3

bS Supporting Information ABSTRACT: Iron is an essential requirement for life for nearly all organisms. The human pathogen Staphylococcus aureus is able to acquire iron from the heme cofactor of hemoglobin (Hb) released from lysed erythrocytes. IsdB, the predominant Hb receptor of S. aureus, is a cell wallanchored protein that is composed of two NEAT domains. The N-terminal NEAT domain (IsdB-N1) binds Hb, and the C-terminal NEAT domain (IsdB-N2) relays heme to IsdA for transport into the cell. Here we present the 1.45 Å resolution X-ray crystal structure of the IsdB-N2
heme complex. While the structure largely conforms to the eight-strand β-sandwich fold seen in other NEAT domains such as IsdA-N and uses a conserved Tyr residue to coordinate heme-iron, a Met residue is also involved in iron coordination, resulting in a novel Tyr-Met hexacoordinate heme-iron state. The kinetics of the transfer of heme from IsdB-N2 to IsdA-N can be modeled as a two-step process. The rate of transfer of heme between the isolated NEAT domains (82 s
1) was found to be similar to that measured for the fulllength proteins. Replacing the iron coordinating Met with Leu did not abrogate high-affinity heme binding but did reduce the heme transfer rate constant by more than half. This unusual Met-Tyr heme coordination may also bestow properties on IsdB that help it to bind heme in different oxidation states or extract heme from hemoglobin.

T

he Gram-positive bacterium Staphylococcus aureus is a common member of the human flora, and colonization with S. aureus primarily results in a commensal relationship with the host.1 Nevertheless, S. aureus is one of the main agents of nosocomial infections and can cause a range of disease, from mild (skin infections such as boils and folliculitis) to severe, lifethreatening bloodstream infections.2 S. aureus possesses a large number of virulence factors that contribute to its ability to cause infection, ranging from secreted toxins and adhesins to strategies for avoiding or subverting the innate and humoral immune responses, as well as the well-documented emergence of antibiotic resistance among increasing numbers of isolates.1,3 In addition to challenges from the innate and acquired immune systems, invading S. aureus must also contend with the nutritional immunity of the human body. Iron is an absolute requirement for diverse cellular processes in the human body, but free iron can destructively react with biological macromolecules; as a result, iron is tightly sequestered within the body.4 During infection, iron sequestration is significantly upregulated through several mechanisms (including enhanced expression of highaffinity iron chelators such as transferrin and lactoferrin) that render biological iron virtually inaccessible to invading pathogens, preventing them from usurping host iron to grow and infect.5 Successful human pathogens have therefore developed mechanisms for accessing sequestered host iron. The most abundant form of iron in the body is in complex with protoporphyrin IX, also known as heme, the majority of which is r 2011 American Chemical Society

bound in the host oxygen-carrier molecule hemoglobin (Hb).4 S. aureus exhibits a preference for heme as an iron source during infection6 and encodes a heme uptake system called the ironresponsive surface determinant (Isd) system, which is able to exploit the heme and hemoprotein resources of the host.7 The Isd system comprises five transcriptional units, each under the control of the Fur repressor, whose repression is relieved under iron-limiting conditions (for a review, see ref 8). The system consists of: four peptidoglycan-anchored surface proteins that can all bind extracellular heme (IsdABCH), a membrane ABC transporter with associated lipoprotein (IsdEF), and two intracellular heme-degrading enzymes (IsdGI). The surface proteins of the Isd system are C-terminally covalently anchored to the peptidoglycan by sortase A (in the case of IsdABH) or sortase B (in the case of IsdC). Furthermore, the surface proteins each contain one to three copies of a conserved protein fold known as a NEAT (for NEAr iron transporter) domain, a fold of ∼125 residues that was identified bioinformatically as being in the genomic neighborhood of putative iron uptake systems.9 Although the degree of sequence identity between NEAT domains can vary wildly, crystal structures of Isd NEAT domains have revealed a common eightstrand β-sandwich fold.10
12 The NEAT domains of the surface Received: March 12, 2011 Revised: May 13, 2011 Published: May 17, 2011 5443

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Figure 1. Schematic of IsdB sequence features. Amino acids are numbered according to the S. aureus N315 IsdB sequence (NP_374246). The black bar near the N-terminus signifies the signal sequence, which directs the protein to be secreted onto the surface. The white bar near the C-terminus signifies the LPQTG sortase signal, which directs the protein to be covalently anchored to the peptidoglycan by sortase A. The two NEAT domains are shown in different shades of gray to indicate their dissimilar pairwise sequence identity (12%). The mature protein on the staphylococcal surface encompasses Ala41
Thr613.

Isd proteins have been further demonstrated to mediate either heme binding10
16 or hemoprotein binding.14,17,18 IsdB contains two NEAT domains9 with 12% pairwise sequence identity and acts as the primary Hb receptor for the cell.19 Deletion of isdB virtually abolishes Hb binding by the S. aureus cell and significantly impacts disease in a mouse infection model.19 IsdB is also highly immunogenic during infection and is the basis for a monovalent vaccine currently undergoing clinical trials.20 IsdB extracts the heme from Hb at the cell surface for the transfer to IsdA or IsdC, which then transfers it to the membrane transporter for internalization.15,21 Recent evidence strongly implies that each NEAT domain of IsdB has a different binding specificity; note that NEAT domain numbering proceeds from the N-terminus to the C-terminus (Figure 1). IsdBN1 binds Hb but not heme.22 Conversely, IsdB-N2 binds heme15,16 but not Hb,22 and its sequence contains a conserved Tyr residue that is known to coordinate the heme-iron in all other heme binding NEAT domains.10
12 IsdB-N2 alone is able to transfer heme to IsdA-N1 and IsdC-N1;15 however, full-length IsdB transfers heme to full-length IsdA at 8 times the rate for fulllength IsdC,21 and protease digestion suggests that IsdB may be physically closer to IsdA than IsdC on the cellular surface,7 suggesting the physiological route of heme transfer is likely from IsdB-N2 to IsdC-N1 via IsdA-N1. We sought to characterize heme binding by IsdB-N2 as a first step in understanding Hb reception and heme transfer by the Isd system. We determined the 1.45 Å resolution crystal structure of heme-bound IsdB-N2 and discovered a new mode of heme-iron coordination, with protein ligands provided by both a Met and a Tyr. We further showed that iron coordination by the Met residue is dispensable for high-affinity heme binding but has a role in facilitating the transfer of heme to IsdA-N1.

’ EXPERIMENTAL PROCEDURES Cloning of NEAT Domains and Variants. The coding region of the second, heme binding NEAT domain (IsdB-N2, Lys341
Thr459) was amplified from S. aureus N315 chromosomal DNA and cloned into the pET28a(þ) expression vector for expression with an N-terminal His6 tag and thrombin cleavage site. Site-directed variants were created by subcloning from the IsdB-N2 clone, using a modified whole plasmid polymerase chain reaction method.23 All clones were verified by sequencing (Agencourt, Beverly, MA). The NEAT domain coding region of IsdA (IsdA-N1, Ser62
Ala184) was subcloned from the previous construct in pET28a, complete with the N-terminal His6 tag and ribosome binding site,10 into pBAD-1824 using the restriction digestion enzymes XbaI and HindIII as previously described.13

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Protein Expression and Purification. Recombinant IsdB-N2 was overexpressed in Escherichia coli BL21(DE3) cells. A 2 L bacterial culture was grown from 2 mL of overnight culture in Luria-Bertani (LB) broth supplemented with 25 μg/mL kanamycin at 30 °C to an OD600 of 0.7
0.9, then induced with 0.5 mM isopropyl β-D-thiogalactopyranoside, and grown for an additional 18 h at 25 °C. Cells were pelleted by centrifugation, resuspended in 20 mL of 20 mM sodium phosphate (pH 7.4) and 500 mM NaCl, and then lysed at 4 °C using an EmulsiFlex-C5 homogenizer (Avestin, Ottawa, ON). Insoluble material was removed by centrifugation; the soluble lysate contained a mixture of apo- and holo-His6-IsdB-N2, and apoprotein could be separated at 4 °C using a HisTrap nickel affinity column (GE Healthcare) by elution with an imidazole gradient. The apoprotein was dialyzed against 50 mM Tris (pH 8.0) and 100 mM NaCl then cleaved with thrombin at a 1:500 ratio by weight of His6-IsdB-N2 to remove the His6 tag. IsdB-N2 was then dialyzed against 50 mM MOPS (pH 7.0) for cation exchange chromatography using a Source 15S column (GE Healthcare), and purified protein was obtained by elution with a NaCl gradient. The resulting pure (>95% by sodium dodecyl sulfate
polyacrylamide gel electrophoresis) apoprotein was dialyzed against either 20 mM Tris (pH 8.0) for crystallization or 50 mM Tris (pH 8.0) and 100 mM NaCl for spectroscopic and kinetic studies. Selenomethionine-labeled (Se-Met) IsdB-N2 was prepared by the method previously described by Van Duyne et al.25 and purified as described for native protein. Heme Reconstitution. Purified apoprotein was incubated for 1 h at 4 °C with 1.5 molar equiv of hemin dissolved in 0.1 M NaOH and diluted in 0.1 M phosphate buffer (pH 7.4). Excess hemin was removed by centrifugation, and nonspecifically bound hemin was removed by gel filtration chromatography on a Sephadex G-50 column (1 cm  6 cm). The concentration of the holoprotein was then determined by the pyridine hemochrome assay using an ε418 extinction coefficient of 191.5 mM
1 cm
1 as previously described.26 Crystal Structure Determination. Native holo-IsdB-N2 and Se-Met IsdB-N2 crystals were grown by hanging drop vapor diffusion at room temperature at a 1:1 ratio of protein to well solution [composed of 0.1 M Tris (pH 8.0), 0.1 M MgCl2, and 25% polyethylene glycol 3350]. Crystals were briefly washed in mother liquor and flash-frozen in liquid nitrogen. Data were collected at the Stanford Synchrotron Radiation Lightsource on beamline 9-2. Data were processed and scaled using HKL2000.27 Crystals grew in space group P212121 with four molecules in the asymmetric unit. Se-Met crystals were generated initially for anomalous phasing, but in the interim, a suitable model was deposited in the Protein Data Bank (PDB) (IsdH-N3, 60% identical; PDB entry 2E7D) and molecular replacement with a single chain (with no heme) from that structure using MolRep28 from the CCP4 program suite29 yielded interpretable phases. Se-Met IsdB-N2 was built using ARPWarp,30 and manual building was completed using Coot.31 A Ramachandran plot revealed that 92.5% of residues were in the most favored regions with the remaining 7.5% in additional allowed regions. Subsequently, native holoIsdB-N2 crystals were generated, and MolRep was again used for phasing by molecular replacement with the Se-Met structure as the search model. The structure was modified using Coot31 and refined with Refmac5.32 Multiple conformations of side chains were modeled by visual examination of Fo
Fc maps. Waters 5444

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Table 1. X-ray Data Collection and Refinement Statistics native

Se-Met

Data Collectiona space group

P212121

P212121

unit cell dimensions

57.5, 82.6, 116.9

52.8, 79.4, 113.9

50.0
1.45

50.0
1.70

a, b, c (Å) resolution range (Å)

(1.50
1.45) Rmerge

0.05 (0.37)

(1.76
1.70) 0.05 (0.31)

I/σI

23.0 (3.9)

24.2 (3.8)

completeness (%) redundancy

99.4 (95.2) 7.1 (5.7)

99.3 (95.5) 4.6 (3.7)

no. of unique reflections

97666

53106

Wilson B (Å2)

18.5

23.6

Refinement Rwork/Rfree

0.178/0.217

no. of atoms

4993

4793

protein/heme

4364

4033

ions water

6 623

5 755

protein

19.5

26.7

heme

15.0

22.8

ions

17.1

23.5

water

28.3

42.0

0.012 1.38

0.013 1.48

0.193/0.232

B factor (Å2)

root-mean-square deviation bond lengths (Å) bond angles (deg) a

Values in parentheses represent those for the highest-resolution shell.

were added using the ARP/Waters30 function in Refmac5, and model quality parameters were assessed using Procheck.33 A Ramachandran plot revealed that 94.3% of residues were in the most favored regions with the remaining 5.7% in additional allowed regions. Figures are of the native structure and were generated using PyMOL.34 Data collection and refinement statistics for both the native and Se-Met IsdB-N2 structures are listed in Table 1. Determination of the IsdB-N2 Heme Binding Stoichiometry. Heme binding was tracked by difference absorption spectroscopy in the Soret region (around 400 nm) at room temperature. Aliquots of hemin (1.3 μL) solubilized in 0.1 M NaOH and diluted in 50 mM Tris (pH 8.0) and 100 mM NaCl were added to 1 mL of a 5 μM solution of apo-IsdB-N2 or a reference cuvette containing buffer alone. Spectra were recorded 10 min after addition of heme, and titrations covered a heme concentration range from 0.5 to 12 μM. Saturation was defined as a plateau in the absorption difference between the reference cuvette and the experimental cuvette. For reference, absorption spectra (250
650 nm) of purified reconstituted proteins were measured. All spectra were recorded using a Cary 50 Bio UV
visible spectrophotometer (Agilent Technologies, Mississauga, ON) with an optical path length of 1 cm in a quartz cell at room temperature. Trp Fluorescence Quenching by Heme. Heme binding was monitored by fluorescence quenching of the tryptophan residue (Trp392) at the base of the heme pocket, based on the method described by Eakanunkul et al.35 Fluorescence emission spectra

from 300 to 450 nm were recorded at 20 °C with excitation at 295 nm in 50 mM Tris (pH 8) and 100 mM NaCl with an apoIsdB-N2 concentration of 1 μM in a 1 mL volume using a Cary Eclipse fluorescence spectrophotometer (Agilent Technologies). Heme (prepared as described above, in various dilutions) was added to the buffered protein solution in 0.5
1.5 μL aliquots and allowed to reach equilibration (which ranged from 6 to 12 min depending on the variant) before readings were taken. The titrations covered a heme concentration range of 0.1
15 μM. The dissociation constant (KD) was calculated from the decrease in the fluorescence intensity between 300 and 450 nm as a function of increasing heme concentration, using an equation for equilibrium binding that accounts for ligand depletion as described by Stein et al.36 All reactions were conducted in triplicate. Determination of Rates of Transfer of Heme to Apomyoglobin. The rates of dissociation of heme from IsdB-N2 were measured by single-wavelength stopped-flow spectroscopy with apomyoglobin (apoMb) as a heme scavenger.37 ApoMb was prepared from myoglobin (Sigma-Aldrich, St. Louis, MO) as previously described.38 Heme dissociation reactions were conducted with 10 μM holo-IsdB-N2 (reconstituted as described above) in one syringe (final concentration of 5 μM) and 100 μM apomyoglobin (final concentration of 50 μM) in the second syringe, both in 50 mM Tris (pH 8) and 100 mM NaCl at room temperature in an SX.18MV stopped-flow reaction analyzer (Applied Photophysics, Leatherhead, U.K.). Reactions were monitored by recording the absorbance at 408 nm for 1000 s (wild-type; ∼7 half-lives) or 600 s (M362L variant; ∼11 halflives); 1000 readings at logarithmic intervals were acquired using Pro-Data SX software, regardless of the time frame. The change in absorbance at 408 nm (maximal absorbance for holomyoglobin) was plotted versus time and fit by a double-exponential equation to yield the first-order rate constants for heme dissociation using GraphPad Prism version 5.02 for Windows (GraphPad Software, La Jolla, CA). All reactions were conducted in triplicate. Determination of Rates of Transfer of Heme to IsdA-N1. Differences in spectral characteristics between holo-IsdB-N2 and holo-IsdA-N1 were exploited to monitor the transfer of heme from holo-IsdB-N2 to apo-IsdA-N1 by stopped-flow spectroscopy, conducted using an SX.18MV stopped-flow reaction analyzer (Applied Photophysics) equipped with a photodiode array detector. The reactions were conducted with 4 μM holoIsdB-N2 in one syringe (final concentration of 2 μM) and concentrations of apo-IsdA-N1 ranging from 20 to 100 μM (final concentrations of 10
50 μM) in the second syringe; a minimal 5-fold excess of the IsdA acceptor was used to attain pseudo-first-order conditions. One hundred spectra were recorded at logarithmic intervals from 0 to 10 s from approximately 300 to 650 nm, using Xscan (Applied Photophysics). The drive syringe chamber and optical cell were maintained at 25 °C by a circulating water bath. The change in absorbance over time at the wavelength of maximal change (418.9 nm for the wild type and 425.3 nm for the M362L variant) for a given concentration was fit by a single-exponential equation to determine the observed transfer rate (kobs). All reactions were conducted in quadruplicate.

’ RESULTS Crystal Structure of IsdB-N2. The holo structure of IsdB-N2 was determined to 1.45 Å resolution. The structure of Se-Met IsdB-N2 was also determined to 1.7 Å but was inappropriate for interpretation of heme binding due to the artifact introduced by 5445

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Figure 2. Crystal structure of the heme-bound C-terminal NEAT domain of IsdB. (A) Overall structure of holo-IsdB-N2 (chain A) viewed down the heme binding pocket. The backbone is shown as a cartoon with helices colored purple, β-strands cyan, and loops gray. Heme is shown protruding from the pocket as sticks, with carbon atoms colored dark blue and oxygen atoms red. One conformation of heme is shown for the sake of clarity. The N- and C-termini and helices are labeled. (B) Close-up of the heme pocket. Residues directly involved in binding the heme molecule (Tyr440, Met362, and Ser361) or indirectly involved in binding (Tyr444) are shown as sticks and labeled. Protein carbon, oxygen, and sulfur atoms are colored purple, red, and yellow, respectively. Heme carbon, oxygen, nitrogen, and iron atoms are colored blue, red, dark blue, and dark red, respectively. (C and D) Fo
Fc omit maps (contoured at 3σ) for Tyr440, Met362, and heme of chains A and B.

the selenomethionine substitution, discussed in a later section. There were four molecules in the asymmetric unit that overlaid with an average root-mean-square deviation (rmsd) of 0.49 Å over all CR atoms, with the main differences occurring at the N-termini. The final model consists of residues 341
452 for chain A, 341
458 for chains B and C, and 341
456 for chain D and includes an N-terminal Gly-Ser cloning artifact left over from the thrombin cleavage site. IsdB-N2 adopts the characteristic eight-strand immunoglobulin-like β-sandwich fold observed in other NEAT domains whose structures are known (Figure 2A).10
12,14,39 In addition to short R-helices between β1 and β2 and between β3 and β4, there is a C-terminal R-helix of approximately 1.5 turns immediately following β8 that is not observed in other NEAT domain structures. Structure of the Heme Binding Pocket. Heme is bound in a highly hydrophobic pocket and is modeled at equal occupancy in two orientations when rotated by 180° along the CR
Cγ axis (Figure 2B). Approximately 330 Å2 (38%) of the heme surface area was found to be exposed to solvent as calculated using AreaIMol.29 Crystal packing interactions occurred across the face

of the heme pocket, resulting in vinyl groups of heme molecules being ∼3.3 Å apart (Figure 1 of the Supporting Information). The heme propionates are extended out from the pocket, and one forms a hydrogen bond with the hydroxyl group of Ser361 and the backbone nitrogen of Met362. Tyr440, Tyr444, and Phe366 contribute to π-stacking with a buried heme pyrrole ring, whereas Val431, Val433, Val446, Val435, Tyr391, Trp392, and Met363 contribute to hydrophobic contacts. The heme iron is coordinated by Tyr440, which forms a hydrogen bond with the phenolate of Tyr444, an interaction that is absolutely conserved among heme binding NEAT domains of known structure.10
12 The heme-iron exists in a mixture of hexacoordinate and pentacoordinate states, with the sulfur from Met362 occupying the sixth-coordinate position. The electron density is best modeled with Met362 in both coordinating and noncoordinating conformations in the structure, and the occupancy of the conformations is unequal and dependent upon the molecule examined. In chains A and D, inspection of Fo
Fc maps indicates that Met362 exists in a coordinating position at 75% occupancy (sulfur atom 2.5
2.6 Å from heme-iron) and 25% occupancy in a noncoordinating position (sulfur atom 5446

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5.0 Å from heme-iron) (Figure 2C). The opposite is true for chains B and C, where the sulfur atom models away from the pocket at 70% occupancy (4.8 Å from heme-iron) and the sulfur atom is directed toward the heme iron at 30% occupancy (2.6 Å from heme-iron) (Figure 2D). Furthermore, these conformations appear to be complementary to one another, such that the heme pocket containing a mainly coordinating Met362 (chain A or D) is tightly packed against a heme pocket containing a mainly noncoordinating Met362 (chain B or C). Lastly, the heme-iron is pulled out of the plane of the porphyrin ring and closer to Tyr440 in chains B and C (2.1
2.2 Å Fe
O bond length, 0.4
0.5 Å from planarity), where Met362 is mainly noncoordinating, whereas the iron is pulled away from Tyr440 and lies closer to the porphyrin ring plane in chains A and D (2.2
2.3 Å Fe
O bond length, less than 0.2 Å from planarity), where Met362 is mainly coordinating. The variability in the Met362 coordination state was first observed in the 1.7 Å Se-Met structure, motivating the determination of the native structure. Although it is well-documented that substitution of a Met heme-iron ligand for Se-Met has little effect on heme iron coordination,40 we were concerned that the slightly larger van der Waals radius of selenium or an incomplete substitution of Se-Met for Met might have caused the mixture of coordination states observed in the structure. Visible Absorption Spectra of Heme Pocket Variants. On the basis of the residues that were seen to directly participate in heme binding in the IsdB-N2 crystal structure, several variants of the wild-type (WT) protein were constructed using site-directed mutagenesis: Y440A, Y444A, S361A, and M362L. The visible absorption spectra of the variants reconstituted with equimolar hemin were compared to that of the WT protein, as the spectrum is indicative of the heme environment. Mutation of any one of these residues was found to significantly affect the shape, height, and maximum wavelength of the Soret peak, indicating a significant change in the environment experienced by the heme (Figure 3A). Furthermore, the spectra of the Y444A, Y440A, and S361A variants more closely resembled that of free heme than that of WT IsdB-N2, indicating that loss of Tyr444, Tyr440, or Ser361 resulted in severe heme binding disruption. The spectrum of M362L resembled most closely that of the wild-type hemoprotein rather than that of free heme, with a less pronounced shoulder at 380 nm and more pronounced R/β bands (Figure 3B). However, the Soret peak shifted from 404 nm for WT to 398 nm for M362L, and the Soret shape and height were also significantly different, indicating different heme environments. Heme Titration of IsdB-N2 and Variants. Although a single heme molecule is bound per monomer of IsdH-N3 in the crystal structure, investigators found that a monomer could bind up to four molecules of heme in solution.12 Though the crystal structure of IsdB-N2 also bound one heme per monomer, to confirm that 1:1 stoichiometry was recapitulated in solution apoprotein was titrated with increasing amounts of heme and difference spectra were generated by subtracting spectra from that of the buffer titrated with the same amounts of heme. WT IsdB-N2 and M362L (Figure 4A,B) both demonstrated a binding stoichiometry of approximately 1:1. However, Y444A, Y440A, and S361A difference spectra did not follow a single-site, specific binding curve and resembled that of a non-heme binding protein, transferrin, indicating aberrant or extremely weak heme binding (data not shown). Because of the apparent weak binding for these variants, they were deemed unsuitable for performing transfer assays.

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Figure 3. Visible spectra of 5 μM holo-IsdB-N2 WT and variants. Heme (5 μM) was added to apoprotein (5 μM) and allowed to reach equilibrium at room temperature. Spectra of heme (5 μM) alone in buffer and heme (5 μM) added to transferrin, a non-heme binding protein, are also shown for comparison. (A) Spectra of all proteins recorded between 250 and 700 nm. The absorbance at 280 nm is similar for all IsdB-N2 proteins (∼14 kDa), whereas that of transferrin (∼80 kDa) is significantly higher; heme absorbs much less at 280 nm. The spectrum in the Soret range (∼400 nm) is noticeably different for most variants, except S361A and Y444A, which are largely indistinguishable. (B) Close-up of the spectra between 400 and 700 nm revealing characteristic markers of the heme-iron environment. Spectra of WT and M362L are most similar to each other, whereas the spectra of Y440A, Y444A, and S361A resemble the spectrum of free heme.

IsdB-N2 contains one Trp residue (W392), which resides at the base of the heme binding pocket. We were able to exploit this fact to develop a fluorescence-based measurement of heme binding as heme addition causes quenching of Trp fluorescence. We observed a concentration-dependent and saturable quenching of Trp fluorescence by both WT IsdB-N2 and the M362L variant (Figure 4C). At a concentration of 1 μM, IsdB-N2 WT and M362L variant had very similar KD values (0.38 ( 0.06 and 0.49 ( 0.09 μM, respectively) when fit to an equation accounting for ligand depletion; however, as we are working at a protein concentration close to the calculated KD (necessarily high for a reproducible fluorescence signal), these values can be considered only an upper bound, with the actual KD likely being lower. We can conclude that both the native form and M362L variant bind heme with high nanomolar or better affinity. By comparison, the variant proteins that exhibited aberrant or weak heme binding by visible spectroscopy required much greater (at least 5-fold higher) heme concentrations for maximal quenching, and curve fitting suggested dissociation constants at least 5-fold higher (data not shown). Rate of Transfer of Heme to Apomyoglobin. The transfer of heme from the binding pockets of IsdB-N2 WT and M362L 5447

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Figure 5. Transfer of heme from IsdB-N2 to apomyoglobin. There is a considerable change in the visible spectrum as heme is released from holo-IsdB-N2 and bound by apomyoglobin (apoMb). (A and B) The increase in absorbance at 408 nm is characteristic of holomyoglobin formation; a plot of the absorbance at 408 nm vs time fits a two-phase association function in which the rate of formation of holomyoglobin is equal to the off rate from IsdB-N2. The dotted black line is a double-exponential curve fit to the data, and the gray band represents the standard error of three replicates for WT and two replicates for M362L. A graph of the residuals is inset and displays a relatively random distribution: (A) IsdB-N2 WT and (B) IsdB-N2 M362L.

Figure 4. IsdB-N2 WT and M362L variant follow a similar heme binding curve. Titration of 5 μM apo-IsdB-N2 wild-type protein (A) or M362L (B) with heme demonstrates a binding stoichiometry of ∼1:1, as the increase in absorbance at respective Soret peaks when compared to heme alone plateaus at approximately 6 μM. (C) Titration of 1 μM apo-IsdB-N2 WT protein (b) or M362L variant (O) with 0.1
15 μM heme results in a decrease in Trp fluorescence with an increasing heme concentration in a one-site specific manner. A graph of the residuals for both curves is inset.

variant to apomyoglobin (apoMb) was followed by visible stopped-flow spectroscopy at 408 nm, the Soret maximum for holomyoglobin. ApoMb has an affinity for heme in the picomolar range,41 does not directly bind to IsdB,19 and has been used to characterize heme binding by Isd proteins previously.21 The rate of transfer of heme to apoMb is independent of the concentration of apoMb; therefore, the observed rate is assumed to be the rate of release of heme (off rate) from IsdB-N2.37 The transfer rate data are best fit by a double-exponential curve, as judged by

the greater randomness of the residual plot than that for a singleexponential curve. The initial fast phase accounted for only 2.8% of the curve for WT and 3.5% for M362L and may represent the presence of a minor extraneous species in solution, such as improperly folded holo-IsdB-N2 or IsdB-N2 with nonspecifically bound surface heme. The slow phase, describing the vast majority of the absorption change, yielded an off rate of 4.8  10
3 s
1 for WT IsdB-N2 (Figure 5A), and the substitution of Met362 with Leu (Figure 5B) increased the off rate by 2.7-fold, to 1.3  10
2 s
1. A summary of kinetic and equilibrium binding characteristics can be found in Table 2. Rate of Transfer of Heme to IsdA-N1. Using stopped-flow spectroscopy, the observed rates (kobs) of transfer of heme from holo-IsdB-N2 to apo-IsdA-N1 were determined by the difference in the Soret region of their visible spectra at the wavelength of maximal change over ∼0.3 s (for WT) or ∼1.0 s (for M362L), equivalent to a minimum of 15 half-lives. The change in absorbance at 418.9 nm (WT) or 425.3 nm (M362L) was plotted versus time and fit by a single exponential to determine a value for the observed rate constant (kobs). The kobs for 2 μM IsdB-N2 was determined under pseudo-first-order conditions for 5448

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Table 2. Kinetic Parameters of Heme Binding and Transfer off rate ( SE (10
3 s
1) KD ( SE (heme; μM)

a

kfast

kslow

ktransfer ( SE (s
1)

KDa ( SE (μM)

IsdB-N2 WT